Progressive external ophthalmoplegia with mitochondrial dna deletions (autosomal dominant)

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Subtype of: Progressive external ophthalmoplegia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Progressive external ophthalmoplegia with mitochondrial DNA deletions (autosomal dominant)
MONDO_0018002
RRM2B Unknown
27604308
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Progressive external ophthalmoplegia with mitochondrial dna deletions (autosomal dominant).
5 View disease cluster →
Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction 1 shared geneRRM2B Related via 1 shared gene including RRM2B. Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 1 shared geneRRM2B Related via 1 shared gene including RRM2B. Mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) 1 shared geneRRM2B Related via 1 shared gene including RRM2B. Chronic progressive external ophthalmoplegia 1 shared geneRRM2B Related via 1 shared gene including RRM2B. Camptocormia 1 shared geneRRM2B Related via 1 shared gene including RRM2B.